A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637546



Internal ID6677650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:153017..163827hg38UCSC Ensembl
chr16:203016..213826hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810811
hg1910811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15354770, essv15354778, essv15354785, essv15354800, essv15354814, essv15354764, essv15354769, essv15354806, essv15354813, essv15354812, essv15354808, essv15354793, essv15354755, essv15354754, essv15354796, essv15354777, essv15354791, essv15354782, essv15354786, essv15354779, essv15354794, essv15354792, essv15354758, essv15354766, essv15354752, essv15354775, essv15354783, essv15354781, essv15354787, essv15354756, essv15354798, essv15354751, essv15354803, essv15354757, essv15354799, essv15354753, essv15354795, essv15354780, essv15354790, essv15354763, essv15354805, essv15354802, essv15354759, essv15354801, essv15354804, essv15354815, essv15354784, essv15354771, essv15354797, essv15354810, essv15354811, essv15354776, essv15354809, essv15354774, essv15354789, essv15354761, essv15354773, essv15354767, essv15354788, essv15354807, essv15354762, essv15354768, essv15354765, essv15354760, essv15354772
SamplesHG01878, HG02138, NA18528, HG01811, HG01817, HG01944, HG01800, HG02088, HG02513, NA19435, HG01845, NA18993, HG00463, NA19317, HG02029, HG02389, HG01844, HG03401, HG04200, NA18965, HG01843, HG02390, NA18624, NA19059, HG02121, NA18622, HG00759, HG01866, HG01851, NA19083, NA19066, NA18976, HG01599, NA19316, HG00867, HG01797, HG02392, HG00844, HG03786, NA18986, HG00560, HG01170, HG01699, HG02384, HG02084, HG01598, HG02190, NA19078, HG00611, HG02154, NA18740, NA20318, HG02186, NA18577, HG01804, HG01619, HG01808, HG00623, HG02399, HG02136, HG00442, NA19092, NA19746, HG01198, HG01870
Known GenesHBZ
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637546
Frequency
Sample Size2504
Observed Gain65
Observed Loss0
Observed Complex0
Frequencyn/a


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